Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 24 | ||
rs174537 | 0.708 | 0.400 | 11 | 61785208 | non coding transcript exon variant | G/T | snv | 0.28 | 23 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 18 | ||
rs174533 | 0.763 | 0.160 | 11 | 61781553 | intron variant | G/A | snv | 0.37 | 0.29 | 18 | |
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 17 | |||
rs174583 | 0.807 | 0.320 | 11 | 61842278 | intron variant | C/T | snv | 0.35 | 16 | ||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 14 | |||
rs174594 | 0.776 | 0.160 | 11 | 61852357 | intron variant | C/A;T | snv | 14 | |||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs174549 | 0.851 | 0.240 | 11 | 61803910 | 5 prime UTR variant | G/A | snv | 0.26 | 12 | ||
rs174541 | 1.000 | 0.080 | 11 | 61798436 | intron variant | T/C | snv | 0.29 | 8 | ||
rs174566 | 0.925 | 0.160 | 11 | 61824890 | intron variant | A/G | snv | 0.34 | 8 | ||
rs174554 | 1.000 | 0.080 | 11 | 61811991 | intron variant | A/G | snv | 0.40 | 0.28 | 7 | |
rs174574 | 1.000 | 0.080 | 11 | 61832870 | intron variant | A/C | snv | 0.55 | 7 | ||
rs3803800 | 0.807 | 0.240 | 17 | 7559652 | missense variant | A/G | snv | 0.70 | 0.64 | 7 | |
rs968567 | 0.851 | 0.240 | 11 | 61828092 | intron variant | C/T | snv | 0.11 | 7 | ||
rs13538 | 1.000 | 0.080 | 2 | 73641201 | missense variant | A/G | snv | 0.21 | 0.31 | 5 | |
rs174528 | 1.000 | 0.080 | 11 | 61776027 | intron variant | T/C | snv | 0.42 | 0.42 | 5 | |
rs174545 | 1.000 | 0.080 | 11 | 61801834 | 3 prime UTR variant | C/A;G | snv | 0.28 | 5 | ||
rs174560 | 1.000 | 0.080 | 11 | 61814292 | non coding transcript exon variant | T/C | snv | 0.30 | 5 | ||
rs97384 | 1.000 | 0.080 | 11 | 61856709 | non coding transcript exon variant | T/C | snv | 0.46 | 5 | ||
rs174530 | 1.000 | 0.080 | 11 | 61779120 | non coding transcript exon variant | A/G | snv | 0.30 | 4 | ||
rs174568 | 1.000 | 0.080 | 11 | 61826344 | missense variant | C/A;T | snv | 0.37 | 4 |